2008
DOI: 10.1002/app.27293
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Synthesis and light‐emitting properties of a novel π‐conjugated poly[di(p‐phenyleneethynylene)‐alt‐ (p‐phenylenecyanovinylene)] containing n‐octyloxy side branches

Abstract: A novel p-conjugated poly[di(p-phenyleneethynylene)-alt-(p-phenylenecyanovinylene)] having n-octyloxy side chains (PPE-C 8 PPE-PPV) was prepared by polymerization of the monomer DEDB with BCN. Chemical structure of the polymer obtained was confirmed by 1 H NMR, FTIR, and EA. PPE-C 8 PPE-PPV had a molecular weight enough to fabricate the electroluminescent (EL) device, and showed a good organosolubility, excellent thermal stability, and film-forming property. In UV absorption and PL spectra in film it showed a … Show more

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Cited by 5 publications
(4 citation statements)
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“…Common Heck reaction could be completed between the active H atom in the vinyl or ethynyl group with aryl halides, but alternating copolymers could be prepared via cross‐coupling polycondensation with bis(triphenylphosphine) dichloropalladium (Pd(PPh 3 ) 2 Cl 2 ) and phase transfer catalyst (BTEAC) 47, 48. In this reaction, deacetonation of the dibutynol intermediate was realized in the presence of alkali 49…”
Section: Resultsmentioning
confidence: 99%
“…Common Heck reaction could be completed between the active H atom in the vinyl or ethynyl group with aryl halides, but alternating copolymers could be prepared via cross‐coupling polycondensation with bis(triphenylphosphine) dichloropalladium (Pd(PPh 3 ) 2 Cl 2 ) and phase transfer catalyst (BTEAC) 47, 48. In this reaction, deacetonation of the dibutynol intermediate was realized in the presence of alkali 49…”
Section: Resultsmentioning
confidence: 99%
“…Thecommonly used strategy to enhance solubility is the introduction of lateral chains to the benzene ring [9].So, the title compound is an important intermediate in synthesizing these polymers. Up to now, only the synthesis of the title compound has been reported [1].But the crystal structure of it has not been reported in open literature. The title compound has asymmetrical molecule.…”
Section: Discussionmentioning
confidence: 99%
“…Monomer 1 was prepared by modifying a procedure described in the literature 24. Typically, in a 100 mL three‐necked round‐bottom flask equipped with a reflux condenser, thermometer and nitrogen gas inlet, 2,5‐di( n ‐decyloxy)‐1,4‐bis(3‐methyl‐3‐hydroxybut‐1‐ynyl)benzene (2.77 g, 5 mmol) and dry toluene (50 mL) were added.…”
Section: Methodsmentioning
confidence: 99%